The combination of thiocolchicoside and dexketoprofen as therapy of choice for myofascial pain syndrome in the acute period

Authors: Tsyurko B.O., Pelepeychenko A.Yu., Raskaley D.V., Kalyuzhny G.V., Makhinya O.V., Clinic of Neurology and Neuroorthopedics, Kyiv, Ukraine


Thiocolchicoside (Muscomed) is actively used in the USA and EU countries and has proven its effectiveness in a multicenter randomized double placebo-controlled study in acute low back pain [4, 5, 8, 9]. The study was conducted between July 1998 and March 2000 at five centers in 149 patients with acute low back pain treated with thiocolchicoside 2 ml twice daily IM for 5 days. The primary outcome measure was the presence of spontaneous pain on the Visual Assessment Scale (VAS). The finger-to-floor test and the use of paracetamol were used as secondary evaluation criteria. Both groups showed improvement in spontaneous pain assessed by the VAS at the end of day 1. Improvement was statistically significant in the thiocolchicoside group on day 3 (p < 0.001). Finger-sex distance significantly decreased on day 5 in the thiocolchicoside group (p < 0.0005 for both). According to the global patient assessment, 76.8% of patients in the thiocolchicoside group rated the treatment as very good (p < 0.0005). Treatment was well tolerated in both groups and no patients were withdrawn from the study due to adverse effects. As a result, it was found that the administration of 4 mg of thiocolchicoside twice a day for 5 days provides an effective and safe treatment of patients with acute low back pain complicated by myofascial pain syndrome.

ARTICLES FROM CATEGORY
Support of educational events. Participation of World Medicine in the First Congress of Optometrists of Ukraine.
Cetirizine is an effective and safe antihistamine (literature review, results of clinical researches)
All-Ukrainian Scientific and Practical Conference “Aspects of Internal Medicine in Wartime 2024"

PROVE YOU ARE A MEDICAL PROFESSIONAL

Attention: This section is intended for healthcare professionals only. If you are not a medical professional, you can return to the main page by clicking the “No” option

CARD-NOTIFICATION OF AN ADVERSE DRUG REACTION AND/OR LACK OF EFFICACY OF THE MEDICINE

INFORMATION ABOUT THE PATIENT

SUSPECTED AR/LE

Suspected AR (describe each clinical manifestation of the AR with dates and times of onset and end and outcome)/Indication of the LE

INFORMATION ABOUT SUSPECTED MEDICINES

INFORMATION ABOUT RELATED MEDICINES

(with the exception of drugs used to correct the effects of AR/LE)
(concomitant diagnoses, laboratory and instrumental studies, allergy history, pregnancy with gestational age, method of conception, pregnancy outcome (if the pregnancy ended, the date of delivery, type of delivery, etc.)

Information about the messenger

INFORMATION ABOUT THE MEDICAL/PHARMACY SPECIALIST

(if not the notifier)

MESSAGE CARD for the patient

to provide the patient and/or his/her representative with information on adverse drug reactions and/or lack of efficacy of the drug

INFORMATION ABOUT THE PATIENT

Information about the suspected medicine

Information on the prescription of the suspected medicinal product

Information about the messenger

Information about the physician, healthcare facility and place of residence of the patient who had an adverse medicine reaction and/or lack of efficacy of the medicine

розробка сайту Estetic web design